Associated Papers
Enhancing rare variant interpretation in inherited arrhythmias through quantitative analysis of consortium disease cohorts and population controls.
Walsh R et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics, 2021
32893267 (PubMed )
Supplement: 41436_2020_946_MOESM2_ESM.xlsx › S13
Ethnic Differences in Genetic Ion Channelopathies Associated with Sudden Cardiac Death: A Systematic Review and Meta-Analysis.
Kong T et al.
Annals of Clinical and Laboratory Science, 2017
Identification of six novel SCN5A mutations in Japanese patients with Brugada syndrome.
Nakajima T et al.
International Heart Journal, 2011
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